Searchable abstracts of presentations at key conferences in endocrinology

ea0032p236 | Clinical case reports – Pituitary/Adrenal | ECE2013

Pleuropericarditis effusion secondary to chronic bromocriptine intake

Belhimer Faiza , Chentli Farida

Introduction: Dopamine agonists are commonly used for the treatment of Parkison’s disease and prolactinomas. Sometimes high doses are needed in mixed pituitary adenomas. This medical treatment usually induces gastrointestinal troubles and/or low blood pressure, and sometimes psychiatric disorders. Pleuropercarditis effusion (PPE) is rarely related to dopamine agonist side effects.Case report: Our aim is to report a man aged 29 years old whose PPE is...

ea0032p715 | Neuroendocrinology | ECE2013

RET codon 618 mutation is the most frequent genotype in saudi families with multiple endocrine neoplasia type 2a and familial medullary thyroid carcinoma

Qari Faiza , Nasser Tariq

Background and objectives: Certain diseases, such as multiple endocrine neoplasia type 2A (MEN2A), MEN2B, familial and sporadic medullary thyroid carcinoma (MTC) and renal dysgenesis are related to abnormalities of the RET protein. Our aim was to evaluate the frequency of RET mutation in ten Saudi families with MEN2A and familial medullary thyroid carcinoma.Design and setting: Cross-sectional prospective study of patients followed up at King Abd...

ea0032p716 | Neuroendocrinology | ECE2013

Neurological manifestations of Vitamin D deficiency, is there any significant clinical correlation?

Qari Faiza , Nasser Tariq

Objective: The objective of this study was to investigate the correlation between the neurological manifestations of Vitamin D deficiency and the levels of 25(OH) D and bone profile.Methods: We conducted a case series study in patients with osteomalacia who were followed up at King Abdulaziz Medical City, Jeddah, between January 2010 and December 2011. We collected information on demographic data, etiological factors for Vitamin D deficiency, clinical pr...

ea0032p961 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Pituitary hyperplasia secondary to primary hypothyroidism in a child with mosaic trisomy 21

Belhimer Faiza , Chentli Farida

Introduction: Pituitary hyperplasia (PH) is relatively a rare condition in children. As in adults, it can be secondary to a long-standing primary hypothyroidism and can sometimes be mistaken with a pituitary macro-adenoma as in the following observation:Case report: Herein, authors describe a girl aged 10 years old sent by her neurosurgeon for pre operative hormonal exploration of a pituitary macro adenoma measuring 13 mm in height. This one was discover...

ea0022p746 | Thyroid | ECE2010

Pheochromocytoma, papillary thyroid carcinoma: new entity

Nasser Tariq , Qari Faiza

A 53 year-old woman presented with labile and difficult to control hypertension on three deferent anti hypertensive medications. Abdominal computed tomography (CT) and Ultrasonography of the thyroid gland showed 1.8 cm thyroid nodule. Fine needle aspiration biopsy of the thyroid nodule revealed papillary thyroid carcinoma. Serum TSH & FT4, calcitonin, CEA, intact PTH and calcium levels were within normal limits. A 24-h urine metanephrines showed significant elev...

ea0032p52 | Adrenal cortex | ECE2013

Adrenal metastases: aetiolgies and outcome

Boutekedjiret Faiza , Bendali Mohammed , Chentli Farida

Introduction: Adrenal metastases used to be rare in endocrinology compared to others adrenal tumours, and deemed to have a dire prognosis. Our aim is to analyze 13 cases in order to study their morphological aspects, their causes, and their outcome.Subjects and method: Thirteen cases were studied over a long period of time (2000–2012). All of them had biological, hormonal, and radiological assessments.Results: We had ten men a...

ea0032p255 | Clinical case reports – Pituitary/Adrenal | ECE2013

Congenital trans-sphenoidal meningocele: an uncommon cause of pituitary insufficiency

Belhimer Faiza , Bey Abderrahim , Chentli Farida

Introduction: Congenital trans-sphenoidal meningocele (TM) is a rare clinical entity. It can be traumatic, congenital or from tumour origin. It results from a defect in the sphenoid bone ontogenesis. In its classical form, the TM is revealed in adults, frequently in women in the fourth or fifth decade by rhinorrhea or cerebrospinal fluid leak through a bony defect in the sphenoid floor. Our aim is to report a case of large TM without rhinorrhea, and as a part of midline abnorm...

ea0026p365 | Adrenal medulla | ECE2011

Pheochromocytoma occurs in Saudi patients with MEN 2A

Nasser Tariq , Karawagh Abdullah , Qari Faiza

Objective: To evaluate pheochromocytoma that occurs in Saudi patients with MEN 2APatients and methods: Of 44 patients belonging to 5 MEN 2A families, 14 (31.8%) presented with pheochromocytoma. The following variables have been studied: clinical and diagnostic data (age, mutation, clinical features, and laboratory studies included measurements of 24-h urinary catecholamines, epinephrine, metanephrine, norepinephrine, dopamine, vanillylmandelic acid, and ...

ea0015p332 | Steroids | SFEBES2008

HIV and adrenal insufficiency

Rathur Haris , Rathur Faiza , Soran Handrean

A 40-year-old male presented with blackouts. This was associated with transient loss of consciousness with complete subsequent recovery. He did not have any warning signs, tongue biting or urinary incontinence. There was no history of alcohol or elicit drug abuse. He was admitted to MAU.Past medical history: HIV diagnosed 18 months previously. Cutaneous and oral Kaposi’s sarcoma successfully treated with chemotherapy. Hepatitis C, asthma.<p clas...

ea0032p553 | Endocrine tumours and neoplasia | ECE2013

Prolactinoma and vestibular schwannoma: a very rare association

Chentli Farida , Belhimeur Faiza , Azzoug Said , Fedala Nora Soumeya

Introduction: The occurrence of primary pituitary tumour and cerebral schwannoma in the same person is very rare. Only few cases have been reported so far. The mechanism of this association is still unclear.Aim: Our aim is to report a man with two different brain tumours: a prolactinoma and a cerebellopontine schwannoma in order to discuss the possible mechanism of multiple neoplasms arising in the same person.Case report: A man ag...